Direct Visualization of Local Spin Transition Behaviors in Thin Molecular Films by Bimodal AFM

Thin films of the molecular spin‐crossover complex [Fe(HB(1,2,4‐triazol‐1‐yl)₃)₂] undergo spin transition above room temperature, which can be exploited in sensors, actuators, and information processing devices. Variable temperature viscoelastic mapping of the films by atomic force microscopy reveals a pronounced decrease of the elastic modulus when going from the low spin (5.2 ± 0.4 GPa) to the high spin (3.6 ± 0.2 GPa) state, which is also accompanied by increasing energy dissipation. This technique allows imaging, with high spatial resolution, of the formation of high spin puddles around film defects, which is ascribed to local strain relaxation. On the other hand, no clustering process due to cooperative phenomena was observed. This experimental approach sets the stage for the investigation of spin transition at the nanoscale, including phase nucleation and evolution as well as local strain effects.     

AFM‐Based Spin‐Exchange Microscopy Using Chiral Molecules

Local magnetic imaging at nanoscale resolution is desirable for basic studies of magnetic materials and for magnetic logic and memories. However, such local imaging is hard to achieve by means of standard magnetic force microscopy. Other techniques require low temperatures, high vacuum, or strict limitations on the sample conditions. A simple and robust method is presented for locally resolved magnetic imaging based on short‐range spin‐exchange interactions that can be scaled down to atomic resolution. The presented method requires a conventional AFM tip functionalized with a chiral molecule. In proximity to the measured magnetic sample, charge redistribution in the chiral molecule leads to a transient spin state, caused by the chiral‐induced spin‐selectivity effect, followed by the exchange interaction with the imaged sample. While magnetic force microscopy imaging strongly depends on a large working distance, an accurate image is achieved using the molecular tip in proximity to the sample. The chiral molecules' spin‐exchange interaction is found to be 150 meV. Using the tip with the adsorbed chiral molecules, two oppositely magnetized samples are characterized, and a magnetic imaging is performed. This method is simple to perform at room temperature and does not require high‐vacuum conditions.     

Engineering On‐Surface Spin Crossover: Spin‐State Switching in a Self‐Assembled Film of Vacuum‐Sublimable Functional Molecule

The realization of spin‐crossover (SCO)‐based applications requires study of the spin‐state switching characteristics of SCO complex molecules within nanostructured environments, especially on surfaces. Except for a very few cases, the SCO of a surface‐bound thin molecular film is either quenched or heavily altered due to: (i) molecule–surface interactions and (ii) differing intermolecular interactions in films relative to the bulk. By fabricating SCO complexes on a weakly interacting surface, the interfacial quenching problem is tackled. However, engineering intermolecular interactions in thin SCO active films is rather difficult. Here, a molecular self‐assembly strategy is proposed to fabricate thin spin‐switchable surface‐bound films with programmable intermolecular interactions. Molecular engineering of the parent complex system [Fe(H₂B(pz)₂)₂(bpy)] (pz = pyrazole, bpy = 2,2′‐bipyridine) with a dodecyl (C₁₂) alkyl chain yields a classical amphiphile‐like functional and vacuum‐sublimable charge‐neutral Fe^II complex, [Fe(H₂B(pz)₂)₂(C₁₂‐bpy)] (C₁₂‐bpy = dodecyl[2,2′‐bipyridine]‐5‐carboxylate). Both the bulk powder and 10 nm thin films sublimed onto either quartz glass or SiO_x surfaces of the complex show comparable spin‐state switching characteristics mediated by similar lamellar bilayer like self‐assembly/molecular interactions. This unprecedented observation augurs well for the development of SCO‐based applications, especially in molecular spintronics.     

Finite Size Effects on the Switching Dynamics of Spin‐Crossover Thin Films Photoexcited by a Femtosecond Laser Pulse

Using ultrafast optical absorption spectroscopy, the room‐temperature spin‐state switching dynamics induced by a femtosecond laser pulse in high‐quality thin films of the molecular spin‐crossover (SCO) complex [Fe(HB(tz)₃)₂] (tz = 1,2,4‐triazol‐1‐yl) are studied. These measurements reveal that the early, sub‐picosecond, low‐spin to high‐spin photoswitching event, with linear response to the laser pulse energy, can be followed under certain conditions by a second switching process occurring on a timescale of tens of nanoseconds, enabling nonlinear amplification. This out‐of‐equilibrium dynamics is discussed in light of the characteristic timescales associated with the different switching mechanisms, i.e., the electronic and structural rearrangements of photoexcited molecules, the propagation of strain waves at the material scale, and the thermal activation above the molecular energy barrier. Importantly, the additional, nonlinear switching step appears to be completely suppressed in the thinnest (50 nm) film due to the efficient heat transfer to the substrate, allowing the system to retrieve the thermal equilibrium state on the 100 ns timescale. These results provide a first milestone toward the assessment of the physical parameters that drive the photoresponse of SCO thin films, opening up appealing perspectives for their use as high‐frequency all‐optical switches working at room temperature.     

Nanomechanical and Charge Transport Properties of Two‐Dimensional Atomic Sheets

The materials properties of graphene and other two‐dimensional atomic sheets are influenced by atomic‐scale defects, mechanical deformation, and microstructures. Thus, for graphene‐based applications, it is essential to uncover the roles of atomic‐scale defects and domain structures of two‐dimensional layers in charge transport properties. This review highlights recent studies of nanomechanical and charge transport properties of two‐dimensional atomic sheets, including graphene, MoS₂, and boron nitrides. Because of intrinsic structural differences, two‐dimensional atomic sheets give rise to unique nanomechanical properties, including a dependence on layer thickness and chemical modification that is in contrast to three‐dimensional continuum media. Mapping of local conductance and nanomechanical properties on a graphene layer can be used to image the domain and microstructures of two‐dimensional atomic layers. This paper also reviews recent experimental and theoretical findings on the role of bending, defects, and microstructures on nanomechanical and transport properties of graphene‐derived materials.     

Direct Imaging of the Induced‐Fit Effect in Molecular Self‐Assembly

Molecular recognition is a crucial driving force for molecular self‐assembly. In many cases molecules arrange in the lowest energy configuration following a lock‐and‐key principle. When molecular flexibility comes into play, the induced‐fit effect may govern the self‐assembly. Here, the self‐assembly of dicyanovinyl‐hexathiophene (DCV6T) molecules, a prototype specie for highly efficient organic solar cells, on Au(111) by using low‐temperature scanning tunneling microscopy and atomic force microscopy is investigated. DCV6T molecules assemble on the surface forming either islands or chains. In the islands the molecules are straight—the lowest energy configuration in gas phase—and expose the dicyano moieties to form hydrogen bonds with neighbor molecules. In contrast, the structure of DCV6T molecules in the chain assemblies deviates significantly from their gas‐phase analogues. The seemingly energetically unfavorable bent geometry is enforced by hydrogen‐bonding intermolecular interactions. Density functional theory calculations of molecular dimers quantitatively demonstrate that the deformation of individual molecules optimizes the intermolecular bonding structure. The intermolecular bonding energy thus drives the chain structure formation, which is an expression of the induced‐fit effect.     

Magnetic Susceptibility Study of Sub‐Pico‐emu Sample Using a Micromagnetometer: An Investigation through Bistable Spin‐Crossover Materials

A promising and original method to study the spin‐transition in bistable spin‐crossover (SCO) materials using a magnetoresistive multiring sensor and its self‐generated magnetic field is reported. Qualitative and quantitative studies are carried out combining theoretical and experimental approaches. The results show that only a small part of matter dropped on the sensor surface is probed by the device. At a low bias‐current range, the number of detected nanoparticles depends on the amplitude of the current. However, in agreement with the theoretical model, the stray voltage from the particles is proportional to the current squared. By changing both the bias current and the concentration of particle droplet, the thermal hysteresis of an ultrasmall volume, 1 × 10^?4 mm³, of SCO particles is measured. The local probe of the experimental setup allows a highest resolution of 4 × 10^?14 emu to be reached, which is never achieved by experimental methods at room temperature.     

Study of mechanical properties,oxygen permeability and AFM topography of zein films plasticized by polyols

The use of plastic for packaging has grown extensively in recent years. In this context, biodegradable films can be a source of energy saving and an important issue for environmental protection. Zein protein (prolamin of corn) is one of the best biopolymers for edible film making and polyols are convenient plasticizers for biopolymers. Polyols (sorbitol, glycerol and mannitol) at three levels (0.5, 0.7 and 1g/g zein) were used as plasticizers and the tensile properties, oxygen permeability (OP) and AFM topography of zein films were studied. Films plasticized by sorbitol had a relatively higher ultimate tensile strength (UTS) than films containing glycerol and mannitol at low levels of plasticizers (0.25, 0.7g/g zein). There was no significant difference between the strain at break values (SB) of films plasticized by sorbitol and glycerol at low levels of plasticizers, while films plasticized by sorbitol had higher SB than the films containing glycerol and mannitol at a high level of plasticizer (1g/g zein). Pure zein films had low oxygen permeability (OP), and increasing the plasticizer level to 0.5g/g zein decreased OP values in films containing sorbitol and glycerol. Films containing sorbitol and mannitol had the lowest and highest OP values, respectively. AFM images were used to evaluate the surface morphology (qualitative parameter) and roughness (quantitative parameter) of zein films. Films plasticized by glycerol had smoother surfaces and a lower roughness parameter (Rq). No relationship between OP values and the roughness of the zein films was observed. Copyright © 2006 John Wiley & Sons, Ltd.     

Mapping the nanomechanical properties of graphene suspended on silica nanoparticles

Using nanoparticles to impart extrinsic rippling in graphene is a relatively new method to induce strain and to tailor the properties of graphene. Here, we study the structure and elastic properties of graphene grown by chemical vapour deposition and transferred onto a continuous layer of SiO₂ nanoparticles with diameters of around 25 nm, prepared by Langmuir–Blodgett technique on Si substrate. We show that the transferred graphene follows only roughly the morphology induced by nanoparticles. The graphene membrane parts bridging the nanoparticles are suspended and their adhesion to the atomic force microscope tip is larger compared to that of supported graphene parts. These suspended graphene regions can be deformed with forces of the order of 10 nN. The elastic modulus of graphene was determined from indentation measurements performed on suspended membrane regions with diameters in the 100 nm range.     

AFM study of the surface morphology of L-CVD SnO2 thin films

In this paper we present the results of Atomic Force Microscopy (AFM) characterisation of the surface morphology of the L-CVD SnO₂ thin films prepared by L-CVD technology and studied after exposure to air, dry air oxidation, and ion beam profiling. The L-CVD SnO₂ thin films after air exposure have a very smooth surface morphology with an average surface roughness (RMS) smaller than 0.5 nm, and average and maximal grain heights of about 1 and 2 nm, respectively. After dry air oxidation the L-CVD SnO₂ thin films exhibit an average surface roughness (RMS), as well as the average and maximal grain height, increased by one order of magnitude. Finally, after the ion beam profiling the L-CVD SnO₂ thin films exhibit an evidently disordered structure with a lot of craters. These experiments showed that the L-CVD SnO₂ thin films exhibit a very high quality surface morphology, what can be useful for solar cells and gas sensors application.     

Temperature‐Controlled High‐Speed AFM: Real‐Time Observation of Ripple Phase Transitions

With nanometer lateral and Angstrom vertical resolution, atomic force microscopy (AFM) has contributed unique data improving the understanding of lipid bilayers. Lipid bilayers are found in several different temperature‐dependent states, termed phases; the main phases are solid and fluid phases. The transition temperature between solid and fluid phases is lipid composition specific. Under certain conditions some lipid bilayers adopt a so‐called ripple phase, a structure where solid and fluid phase domains alternate with constant periodicity. Because of its narrow regime of existence and heterogeneity ripple phase and its transition dynamics remain poorly understood. Here, a temperature control device to high‐speed atomic force microscopy (HS‐AFM) to observe dynamics of phase transition from ripple phase to fluid phase reversibly in real time is developed and integrated. Based on HS‐AFM imaging, the phase transition processes from ripple phase to fluid phase and from ripple phase to metastable ripple phase to fluid phase could be reversibly, phenomenologically, and quantitatively studied. The results here show phase transition hysteresis in fast cooling and heating processes, while both melting and condensation occur at 24.15 °C in quasi‐steady state situation. A second metastable ripple phase with larger periodicity is formed at the ripple phase to fluid phase transition when the buffer contains Ca²⁺. The presented temperature‐controlled HS‐AFM is a new unique experimental system to observe dynamics of temperature‐sensitive processes at the nanoscopic level.     

Substrate Templating upon Self‐Assembly of Hydrogen‐Bonded Molecular Networks on an Insulating Surface

Molecular self‐assembly on insulating surfaces, despite being highly relvant to many applications, generally suffers from the weak molecule–surface interactions present on dielectric surfaces, especially when benchmarked against metallic substrates. Therefore, to fully exploit the potential of molecular self‐assembly, increasing the influence of the substrate constitutes an essential prerequisite. Upon deposition of terephthalic acid and trimesic acid onto the natural cleavage plane of calcite, extended hydrogen‐bonded networks are formed, which wet the substrate. The observed structural complexity matches the variety realized on metal surfaces. A detailed analysis of the molecular structures observed on calcite reveals a significant influence of the underlying substrate, clearly indicating a substantial templating effect of the surface on the resulting molecular networks. This work demonstrates that choosing suitable molecule/substrate systems allows for tuning the balance between intermolecular and molecule–surface interactions even in the case of typically weakly interacting insulating surfaces. This study, thus, provides a strategy for deliberately exploiting substrate templating to increase the structural variety in molecular self‐assembly on a bulk insulator at room temperature.